The US Food and Drug Administration Commissioner Stephen Hahn defended the agency’s decision making during the COVID-19 pandemic as being rooted in “good data and sound science,” while acknowledging that it has made risk-benefit decisions on medical products using “data sets that might not be as robust as they would under normal circumstances.”
In a speech given over teleconference to the Alliance For A Stronger FDA on Monday, Hahn also said that FDA is “constantly reevaluating” these types of fast decisions and adjusting them as new information become available
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